4000‐8000‐Å Emission from Far‐Ultraviolet Photolysis of N2O, NO, NO2, CO, CO2, and O2
Author:
Publisher
AIP Publishing
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://aip.scitation.org/doi/pdf/10.1063/1.1669017
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3. Intense Resonance Line Sources for Photochemical Work in the Vacuum Ultraviolet Region
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5. Photoionization of n‐Butane at 1067–1048 Å. Decomposition of the Parent Ion and Superexcited Molecule
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1. The influence of Rydberg states on the photodissociation of nitrous oxide;Journal of Physics B: Atomic, Molecular and Optical Physics;2008-07-04
2. Vibrational-state distribution of nitrogen(B3.PI.g) produced from the argon(3P2,0) + nitrous oxide reaction;The Journal of Physical Chemistry;1988-05
3. Collisional deactivation of vibrationally hot ethylene produced by the photoactivation of ethyl bromide at 121.6 nm;Journal of Photochemistry and Photobiology A: Chemistry;1988-03
4. Effectiveness of the scavenging action of NO in vacuum UV photolyses of C2H5Br: 121.6 - 193.1 nm region;Journal of Photochemistry;1987-09
5. Photoexcitation of NO at 1576 Å;The Journal of Chemical Physics;1984-11
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